1,772 results on '"Wynn R"'
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152. HLA-DR15 and survival in HLA identical haemopoietic stem cell transplantation (HSCT): P-280
153. Intractable diarrhoea of infancy caused by neutrophil specific granule deficiency and cured by stem cell transplantation
154. Cross-talk between Thiamin Diphosphate Binding and Phosphorylation Loop Conformation in Human Branched-chain α-Keto Acid Decarboxylase/Dehydrogenase
155. Structural and Biochemical Basis for Novel Mutations in Homozygous Israeli Maple Syrup Urine Disease Patients: A PROPOSED MECHANISM FOR THE THIAMIN-RESPONSIVE PHENOTYPE
156. Expression of E1 Component of Human Branched-Chain α-Keto Acid Dehydrogenase Complex in Escherichia coli by Cotransformation with Chaperonins GroEL GroES
157. Production of Recombinant Mammalian Holo-E2 and E3 and Reconstitution of Functional Branched-Chain α-Keto Acid Dehydrogenase Complex with Recombinant E1
158. Effects of spatially variable intake on surface irrigation advance
159. Mass wasting along the NW African continental margin
160. Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future
161. Association between adenovirus viral load and mortality in pediatric allo-HCT recipients: the multinational AdVance study
162. Comparison of two self administered psychiatric questionnaires (GHQ-12 and SRQ-20) in primary care in Chile
163. Best management of pesticide — furrow irrigation systems
164. Sequential reduced- and full-intensity allografting using same donor in a child with chronic granulomatous disease and coexistent, significant comorbidity
165. Reduced-intensity conditioning in first and second allograft in children without immunodeficiency: experience of three British transplant centres
166. Systemic juvenile idiopathic arthritis, Kikuchiʼs disease and haemophagocytic lymphohistiocytosis
167. Molecular basis of maple syrup urine disease and stable correction by retroviral gene transfer
168. Association of acute parvovirus B19 infection with new onset of acute lymphoblastic and myeloblastic leukaemia
169. Systemic juvenile idiopathic arthritis, Kikuchiʼs disease and haemophagocytic lymphohistiocytosis—is there a link? Case report and literature review
170. Water-demand function
171. Validation and calibration of UCA Model
172. In vitro reconstitution of the 24-meric E2 inner core of bovine mitochondrial branched-chain alpha-keto acid dehydrogenase complex: requirement for chaperonins GroEl and GroES
173. Sickle cell disease: An international survey of results of HLA-identical sibling hematopoietic stem cell transplantation
174. Prominent dyserythropoiesis in four cases of haemophagocytic lymphohistiocytosis
175. Refractory hyperhaemolysis in a patient with β-thalassaemia major
176. The hydrophobic core of Escherichia coli thioredoxin shows a high tolerance to nonconservative single amino acid substitution
177. Determination of red cell volume in infants needing blood transfusion
178. AGGRESSIVE MULTIPLE MODALITY THERAPY FOR VARICELLA-ASSOCIATED PURPURA FULMINANS
179. ASSESSMENT OF A FLOW CYTOMETRIC ASSAY FOR THE DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A PAEDIATRIC HAEMATOLOGY LABORATORY.
180. REFRACTORY HYPERHAEMOLYSIS IN A PATIENT WITH β-THALASSAEMIA MAJOR.
181. Telomere shortening in leucocyte subsets of long-term survivors of allogeneic bone marrow transplantation
182. 'Guttas Campus' - participants' experiences of a group-based intervention to prevent school dropout.
183. PRO146 HEALTH-RELATED QUALITY OF LIFE AND PRODUCTIVITY/ACTIVITY IMPAIRMENT IN PATIENTS WITH TRANSFUSION DEPENDENT B-THALASSAEMIA IN THE UK NHS: DATA FROM A UK MULTICENTRE OBSERVATIONAL STUDY
184. Clinical Implementation and Validation of MR-only planning in Adaptive RT
185. A Team Approach to Commissioning Online MRI-Guided Adaptive Radiotherapy
186. Paroxysmal cold haemoglobinuria of childhood: a review of the management and unusual presenting features of six cases
187. The C-terminal Hinge Region of Lipoic Acid-bearing Domain of E2b Is Essential for Domain Interaction with Branched-chain α-Keto Acid Dehydrogenase Kinase
188. Gender differences in the earnings of lawyers.
189. Flow cytometric determination of pre-transfusion red cell volume in fetuses and neonates requiring transfusion based on RhD sup + dilution by transfused D sup - red cells
190. Molecular and Biochemical Basis of Intermediate Maple Syrup Urine Disease: Occurrence of Homozygous G245R and F364C Mutations at the E1alpha Locus of Hispanic-Mexican Patients
191. Morphostructure, tectono-sedimentary evolution and seismic potential of the Horseshoe Fault, SW Iberian Margin
192. Diagnosis and severity criteria for sinusoidal obstruction syndrome/veno-occlusive disease in pediatric patients: A new classification from the European society for blood and marrow transplantation
193. AUTOIMMUNE & INFLAMMATORY NMD: EP.15 Severe Guillain-Barre syndrome associated with nelarabine with good prognosis
194. Biochemical Basis of Type IB (E1β) Mutations in Maple Syrup Urine Disease: A PREVALENT ALLELE IN PATIENTS FROM THE DRUZE KINDRED IN ISRAEL
195. Roles of Active Site and Novel K+ Ion-binding Site Residues in Human Mitochondrial Branched-chain α-Ketoacid Decarboxylase/Dehydrogenase
196. G-CSF Vs Haematopoietic Stem Cell Transplantation in Severe Congenital Neutropenia with ELANE Mutation: Role of G-CSF Dose. a Retrospective Controlled Study on Behalf of Saawp (Severe Aplastic Anemia Working Party) of the EBMT, of the Stem Cell Transplant for Immunodeficiency Group in Europe (SCETIDE), of the Severe Chronic Neutropenia French Registry (SCNFR) and Italian Neutropenia Registry (INR)
197. Tetrameric Assembly and Conservation in the ATP-binding Domain of Rat Branched-chain α-Ketoacid Dehydrogenase Kinase
198. Crystal structure of human branched-chain α-ketoacid dehydrogenase and the molecular basis of multienzyme complex deficiency in maple syrup urine disease
199. The structure of importin α and the nuclear localization peptide of ChREBP, and small compound inhibitors of ChREBP-importin α interactions.
200. Refining the phenotype associated with biallelic DNAJC21 mutations
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